Medical Device Manufacturer · US , Peabody , MA

Anrad Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Recent clearances: GR17 DIGITAL DETECTOR, DIGITAL DETECTOR, MODEL GR17

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Anrad Corp. Radiology ✕

2 devices

1-2 of 2

Cleared Aug 25, 2005

GR17 DIGITAL DETECTOR

Radiology · 20d

Cleared Oct 22, 2004

DIGITAL DETECTOR, MODEL GR17

Radiology · 10d

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Sep 25, 2026